JPH10158518A - Silicone rubber composition for automobile joint cover - Google Patents

Silicone rubber composition for automobile joint cover

Info

Publication number
JPH10158518A
JPH10158518A JP8321557A JP32155796A JPH10158518A JP H10158518 A JPH10158518 A JP H10158518A JP 8321557 A JP8321557 A JP 8321557A JP 32155796 A JP32155796 A JP 32155796A JP H10158518 A JPH10158518 A JP H10158518A
Authority
JP
Japan
Prior art keywords
weight
parts
organopolysiloxane
unsaturated hydrocarbon
aliphatic unsaturated
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP8321557A
Other languages
Japanese (ja)
Inventor
Kazuma Momii
一磨 籾井
Masaharu Takahashi
政晴 高橋
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Shin Etsu Chemical Co Ltd
Original Assignee
Shin Etsu Chemical Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Shin Etsu Chemical Co Ltd filed Critical Shin Etsu Chemical Co Ltd
Priority to JP8321557A priority Critical patent/JPH10158518A/en
Publication of JPH10158518A publication Critical patent/JPH10158518A/en
Pending legal-status Critical Current

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  • Steering Controls (AREA)
  • Diaphragms And Bellows (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PROBLEM TO BE SOLVED: To obtain the subject composition excellent in the characteristics of bending fatigue resistance and stretching fatigue resistance by compounding a specified organopolysiloxane, a specified organohydrogenpolysiloxane, etc. SOLUTION: This composition is composed of (A) 100 pts.wt. of an organopolysiloxane expressed by average composition formula I [R is a (substituted) monovalent hydrocarbon; (a)=1.95-2.05] and containing at least two aliphatic unsaturated hydrocarbon groups in a molecule, (B) an organohydrogenpolysiloxane expressed by formula II [A is H or R; B is SiRH2 , SiR2 H, etc.; (m)>=0, (n)>=0 and 5<=(m+n)<=100] and containing at least two H atoms bonding to a silicon atom in a molecule in such an amount that the molar ratio of H atoms in the component B to the aliphatic unsaturated hydrocarbon groups in the component A becomes 1.0-2.5, (C) 10-100 pts.wt. of reinforcing silica and (D) a platinum-based catalyst in a catalytic amount.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は自動車のジョイント
カバーブーツ用シリコーンゴム組成物に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a silicone rubber composition for an automobile joint cover boot.

【0002】[0002]

【従来の技術】シリコーンゴムは耐熱性、耐寒性、耐候
性、電気絶縁性、耐圧縮永久歪、ゴム弾性にすぐれてお
り、さらには毒性がないため、電気・電子部品、事務用
機器、自動車、航空機などの部品、食品製造装置部品、
医療器具部品からレジャー用品まで広範囲で使用されて
おり、これらは静的用途だけでなく、電卓、プッシュホ
ンなどにおけるラバーコンタクト、キーボード、自動車
の等速ジョイントカバーブーツ、ダイヤフラム、医療用
ポンプチューブなどのような動的用途にも多く使用され
ている。しかし、このシリコーンゴムも動的用途におい
ては耐伸長、耐屈曲疲労特性が必ずしも満足する結果を
示さないので、これらに対する対策として一般の合成ゴ
ムの耐動的疲労特性の向上のために用いられている均一
架橋、低架橋密度、低モジュラス、充填剤についてはそ
れらの使用量の減少化、均一分散化、粗粒充填剤の除去
などの手段が適宜採用されているが、このような方法で
はその耐伸長、耐屈曲疲労特性の向上が不十分でった。
即ち最も一般的なデマッシャ式疲労テスト法で 300〜 4
00万回レベルが限界であったので、これら特性の改良が
強く求められている。また、この耐疲労特性向上につい
てはこれ以外に、オルガノハイドロジエンポリシロキサ
ンを添加する方法(特開昭62-197454 号公報参照)、フ
ッ素含有低分子量重合体を添加する方法(特開昭63-150
350 号公報参照)も提案されている。
2. Description of the Related Art Silicone rubber is excellent in heat resistance, cold resistance, weather resistance, electrical insulation, compression set and rubber elasticity, and has no toxicity. , Aircraft parts, food production equipment parts,
It is used in a wide range of applications, from medical device parts to leisure goods, such as rubber contacts in calculators, touch phones, keyboards, constant velocity joint cover boots for automobiles, diaphragms, medical pump tubes, etc. It is often used for various dynamic applications. However, this silicone rubber does not always show satisfactory results of elongation resistance and bending fatigue resistance in dynamic applications, and is used as a measure against these to improve the dynamic fatigue resistance of general synthetic rubber. As for uniform crosslinking, low crosslinking density, low modulus, and filler, means such as reduction of the amount used, uniform dispersion, and removal of coarse-grained filler are appropriately adopted. The improvement of elongation and bending fatigue resistance was insufficient.
In other words, the most common Demasher type fatigue test method is 300 to 4
Since the millionth level was the limit, improvement of these characteristics has been strongly demanded. Other methods for improving the fatigue resistance include a method of adding an organohydrogenpolysiloxane (see JP-A-62-197454) and a method of adding a fluorine-containing low-molecular-weight polymer (see JP-A-63-197454). 150
No. 350) has also been proposed.

【0003】[0003]

【発明が解決しようとする課題】しかし前記の方法のみ
では、耐伸長疲労特性には優れるが JIS K6301の屈曲試
験にあるような、予めクラックがある物体の圧縮疲労に
よる亀裂の成長においては、著しく寿命が短い組成物も
あり、自動車のブーツ材の様な繰返し圧縮と伸長を受け
る構造物の材料には不適当であった。
However, the above method alone is excellent in elongation fatigue resistance, but is remarkable in crack growth due to compression fatigue of an object having a crack in advance, as in the bending test of JIS K6301. Some compositions have short lifespans and are unsuitable for materials of structures that are subject to repeated compression and expansion, such as automotive boot materials.

【0004】本発明はこのような問題点を解決した耐屈
曲疲労特性、特にクラックの成長速度の非常に遅い、且
つ耐伸長疲労特性に優れた自動車ジョイントカバーブー
ツ用のシリコーンゴム組成物を提供する。
[0004] The present invention provides a silicone rubber composition for automobile joint cover boots which solves the above-mentioned problems and has excellent bending fatigue resistance, in particular, very low crack growth rate and excellent extension fatigue resistance. .

【0005】[0005]

【課題を解決するための手段】本発明は下記イ)、
ロ)、ハ)、ニ)からなる自動車ジョイントカバーブー
ツ用シリコーンゴム組成物である。 イ)平均組成式RaSiO(4-a)/2で示され、1分子中に少なくとも2個の脂肪族不飽 和炭化水素基を有するオルガノポリシロキサン 100重量部、 (但し式中Rは置換または非置換の一価炭化水素基で、aは1.95〜2.05の正数) ロ)下記一般式(化2)で示され、1分子中にケイ素原子に結合した水素原子を 少なくとも2個有するオルガノハイドロジエンポリシロキサン 「但しロ)の 水素原子のモル数とイ)の脂肪族不飽和炭化水素基のモル数との比が 1.0〜2.5 となる重量部」、 「式中R は前記と同じ,A はH またはR ,B はSiRH2,SiR2H,SiR3から選ばれる基 ,mはm≧0の整数,nはn≧0の整数で且つ5≦(m+n)≦100 」
Means for Solving the Problems The present invention provides the following a),
A silicone rubber composition for automotive joint cover boots comprising (b), (c) and (d). B) 100 parts by weight of an organopolysiloxane represented by the average composition formula R a SiO (4-a) / 2 and having at least two aliphatic unsaturated hydrocarbon groups in one molecule, wherein R is A is a substituted or unsubstituted monovalent hydrocarbon group, a is a positive number from 1.95 to 2.05) b) is represented by the following general formula (Chemical Formula 2) and has at least two hydrogen atoms bonded to a silicon atom in one molecule Organohydrogenpolysiloxane "where the ratio of the number of moles of hydrogen atoms in b) to the number of moles of aliphatic unsaturated hydrocarbon groups in b) is 1.0 to 2.5", wherein R is the same as defined above. , a is H or R, B is SiRH 2, SiR 2 H, a group selected from SiR 3, m is an integer of m ≧ 0, n is and 5 ≦ an integer n ≧ 0 (m + n) ≦ 100 "

【化2】 ハ)補強性シリカ 10〜 100重量部、 ニ)白金系触媒 触媒量。 即ち、本発明者らは白金触媒による付加加硫型のシリコ
ーンゴム組成物の成形品は亀裂の成長速度が遅く且つ耐
伸長疲労特性に優れるものであり、特に自動車のジョイ
ントブーツ材に適することを見出し本発明を完成した。
特に本発明の組成物からなる成形品等は100 %伸長疲労
寿命が400 万回を超え、且つ予めクラックの生じた物体
の屈曲テストにおいてクラックが2倍となる屈曲回数が
4万回以上という優れた特性を有している。
Embedded image C) Reinforcing silica 10 to 100 parts by weight, d) Platinum catalyst Catalyst amount. That is, the present inventors have found that a molded article of an addition-vulcanization-type silicone rubber composition using a platinum catalyst has a low crack growth rate and excellent elongation fatigue resistance, and is particularly suitable for a joint boot material of an automobile. The present invention has been completed.
In particular, molded articles made of the composition of the present invention have an excellent 100% elongation fatigue life of more than 4 million times, and the number of times of bending at which a crack doubles in a bending test of a previously cracked object is 40,000 times or more. It has characteristics.

【0006】[0006]

【発明の実施の形態】本発明におけるイ)成分のオルガ
ノポリシロキサンは従来から室温硬化型あるいは加熱硬
化型のシリコーンゴムの主原料として公知のものでよ
く、平均組成式がRaSiO(4-a)/2で示され、1分子中に少
なくとも2個の脂肪族不飽和炭化水素基を有する。ここ
でRは炭素数1〜10、好ましくは炭素数1〜8の置換ま
たは非置換の一価炭化水素基で、メチル、エチル、プロ
ピル、ブチルなどのアルキル基;ビニル、アリルなどの
アルケニル基;フェニル、トリルなどのアリール基;シ
クロヘキシル基などのシクロアルキル基;ベンジル、β
- フェニルエチルなどのアラルキル基またはこれらの基
の炭素原子に結合した水素原子の一部または全部をハロ
ゲン原子、シアノ基などで置換した3,3,3−トリフ
ロロプロピル基、クロロメチル基、シアノエチル基など
から選択されるものであり、aは1.95〜2.05の正数であ
る、基本的に直鎖状のジオルガノポリシロキサンである
が、一部に分枝状の構造を含むものでもよい。
BEST MODE FOR CARRYING OUT THE INVENTION The organopolysiloxane of component (a) in the present invention may be any of those conventionally known as main raw materials for room-temperature-curable or heat-curable silicone rubbers, and has an average composition formula of R a SiO (4- a) / 2 , having at least two aliphatic unsaturated hydrocarbon groups in one molecule. Here, R is a substituted or unsubstituted monovalent hydrocarbon group having 1 to 10 carbon atoms, preferably 1 to 8 carbon atoms, such as an alkyl group such as methyl, ethyl, propyl and butyl; an alkenyl group such as vinyl and allyl; Aryl groups such as phenyl and tolyl; cycloalkyl groups such as cyclohexyl group; benzyl, β
-Aralkyl groups such as phenylethyl, or 3,3,3-trifluoropropyl, chloromethyl, cyanoethyl in which part or all of the hydrogen atoms bonded to the carbon atoms of these groups are substituted with halogen atoms, cyano groups, etc. A is a positive number from 1.95 to 2.05, and is basically a linear diorganopolysiloxane, but may have a partially branched structure.

【0007】本発明におけるオルガノポリシロキサンは
低重合度の液状物であってもよいが、本発明の組成物か
ら得られる硬化弾性体が実用的な硬度を有することが要
求されるので、平均重合度が 300以上の重合体が好まし
く、シリコーン組成物を液状とする場合は重合度300 〜
3,000 、ミラブルとする場合は重合度3,000 〜10,000と
するのが好ましい。Rについては、50モル%以上がメチ
ル基であることが好ましく、ビニル基については0.01〜
5モル%含むことが好ましく、0.02〜5モル%含有する
ことが更に好ましい。
The organopolysiloxane in the present invention may be a liquid having a low degree of polymerization, but the cured elastomer obtained from the composition of the present invention is required to have a practical hardness. A polymer having a degree of polymerization of 300 or more is preferable.
In the case of 3,000 or millable, the degree of polymerization is preferably 3,000 to 10,000. About R, it is preferable that 50 mol% or more is a methyl group, and about 0.01 to
It is preferably contained in an amount of 5 mol%, more preferably 0.02 to 5 mol%.

【0008】上記オルガノポリシロキサンにおいて、R
の脂肪族不飽和炭化水素基の含有率の異なる2種のオル
ガノポリシロキサンを混用することが耐伸長疲労性向上
のために好ましく、特に分子鎖末端が脂肪族不飽和基で
あり、Rの 0.25 〜10モル%(好ましくは0.5 〜5モル
%)が不飽和炭化水素基であるオルガノポリシロキサン
を0.5 〜30重量%[イ)のオルガノポリシロキサン100
重量部中0.5 〜30重量部]含有することが好ましい。残
りは両末端がジメチルビニルシロキシ基で封鎖されたジ
メチルポリシロキサンであることが好ましい。
In the above organopolysiloxane, R
It is preferable to mix two types of organopolysiloxanes having different aliphatic unsaturated hydrocarbon group contents in order to improve the elongation fatigue resistance. In particular, the terminal of the molecular chain is an aliphatic unsaturated group, and R is 0.25. 1010 mol% (preferably 0.5〜5 mol%) of an organopolysiloxane having an unsaturated hydrocarbon group is 0.53030% by weight [A] of organopolysiloxane 100
0.5 to 30 parts by weight in weight parts]. The remainder is preferably dimethylpolysiloxane having both ends blocked with a dimethylvinylsiloxy group.

【0009】本発明におけるロ)のオルガノハイドロジ
エンポリシロキサンは1分子中にケイ素原子に結合した
水素原子を少なくとも2個有するオルガノハイドロジエ
ンポリシロキサンであって、一般式(化1)において重
合度(m+n)が5〜100 、好ましくは10〜30であり、
且つ1分子中のケイ素原子に結合した水素原子のモル数
とイ)のオルガノポリシロキサン1分子中に含有される
不飽和炭化水素基のモル数との比が 1.0〜2.5 、好まし
くは 1.5〜2.0 の範囲となる量を使用する。重合度が5
未満であっても、100 を超えても耐屈曲疲労特性が不十
分となる。またモル比が 1.0未満では硬化したゴムの物
性及び耐伸長疲労性が低下し、2.5 を超えると屈曲によ
る亀裂の成長速度が大きくなる。上記 1.0〜2.5 の範囲
内にあれば、耐伸長疲労性の改善及び亀裂成長抑制の効
果が顕著に現れる。
The organohydrogenpolysiloxane (b) in the present invention is an organohydrogenpolysiloxane having at least two hydrogen atoms bonded to a silicon atom in one molecule. m + n) is from 5 to 100, preferably from 10 to 30,
And the ratio of the number of moles of hydrogen atoms bonded to silicon atoms in one molecule to the number of moles of unsaturated hydrocarbon groups contained in one molecule of the organopolysiloxane a) is 1.0 to 2.5, preferably 1.5 to 2.0. Use an amount in the range of Polymerization degree is 5
If it is less than 100 or more than 100, the bending fatigue resistance becomes insufficient. If the molar ratio is less than 1.0, the physical properties and elongation fatigue resistance of the cured rubber are reduced, and if it exceeds 2.5, the growth rate of cracks due to bending increases. When it is in the range of 1.0 to 2.5, the effects of improving the elongation fatigue resistance and suppressing the crack growth are remarkably exhibited.

【0010】本発明におけるハ)の補強性シリカは煙霧
質シリカ、沈降性シリカ、シリカアエロゲルなど従来か
らシリコーンゴムの充填剤として公知のものでよく、こ
れはゴムに補強性を付与するものであるから比表面積が
50m2/g 以上、特に 150m2/g以上が好ましく、更に好ま
しくは比表面積200 m2/g以上の煙霧質シリカである。ま
たこのシリカはその表面をクロルシラン、アルコキシシ
ラン、シランカップリング剤、シロキサン、シラザン等
で処理したものでもよく、その配合量はイ)のオルガノ
ポリシロキサン 100重量部に対して10重量部未満ではそ
の補強効果が不充分となり、 100重量部を超えるとゴム
の加工性が著しく悪化するので10〜 100重量部の範囲と
する必要があるが、好ましい範囲は20〜70重量部であ
る。
The reinforcing silica (c) in the present invention may be any of those conventionally known as silicone rubber fillers such as fumed silica, precipitated silica, silica aerogel and the like, which imparts reinforcing properties to the rubber. Because there is a specific surface area
50 m 2 / g or more, particularly 150 meters 2 / g or more is preferable, more preferably a specific surface area of 200 m 2 / g or more fumed silica. The silica may be one whose surface is treated with chlorosilane, alkoxysilane, silane coupling agent, siloxane, silazane or the like. The compounding amount is less than 10 parts by weight per 100 parts by weight of the organopolysiloxane of a). If the reinforcing effect is insufficient, and if it exceeds 100 parts by weight, the processability of the rubber is remarkably deteriorated. Therefore, it is necessary to set the range of 10 to 100 parts by weight, but the preferable range is 20 to 70 parts by weight.

【0011】本発明におけるニ)の白金系触媒として
は、白金黒、アルミナ、シリカなどの担体に固体白金を
担持させたもの、塩化白金酸、アルコール変性塩化白金
酸、塩化白金酸とオレフィンとの錯体、白金とビニルシ
ロキサンとの錯体が例示される。これらの白金系触媒の
使用量は触媒量でよいが通常、イ)のオルガノポリシロ
キサン 100重量部あたり、白金元素換算で 0.1〜2,000p
pm、特に 0.5〜200ppmの割合で配合するのが好適であ
る。また、白金系触媒を使用した付加反応においてポッ
トライフを維持するための制御剤、例えばアセチレンア
ルコール等を加えることは任意である。
The platinum-based catalyst according to the present invention d) includes solid platinum supported on a carrier such as platinum black, alumina or silica, chloroplatinic acid, alcohol-modified chloroplatinic acid, or chloroplatinic acid and olefin. Examples of the complex include a complex of platinum and vinyl siloxane. The amount of the platinum-based catalyst used may be a catalytic amount, but is usually 0.1 to 2,000 p in terms of platinum element per 100 parts by weight of the organopolysiloxane of a).
It is preferable to mix at a ratio of pm, especially 0.5 to 200 ppm. It is optional to add a control agent for maintaining the pot life in the addition reaction using a platinum-based catalyst, for example, acetylene alcohol.

【0012】本発明のシリコーンゴム組成物は上記イ)
〜ニ)の所定量を均一に混合することによって得られる
が、この混合方法は一般のシリコーンゴム組成物の配合
に使用される2本ロール、ニーダー、バンバリーミキサ
ーなどで混練すればよく、この際、耐熱性向上剤として
の金属酸化物、着色剤、加工助剤などを添加することは
任意であり、これにはさらに下記一般式(化3)で表さ
れる有機ケイ素化合物をシリカ分散剤として前記イ)成
分のオルガノポリシロキサン 100重量部に対して、10重
量部以下、好ましくは 0.5〜10重量部添加してもよい。
The silicone rubber composition of the present invention has the above-mentioned a)
This method can be obtained by uniformly mixing a predetermined amount of the above (2) to (4), which may be kneaded with a two-roll mill, a kneader, a Banbury mixer or the like used for compounding a general silicone rubber composition. It is optional to add a metal oxide as a heat resistance improver, a coloring agent, a processing aid, and the like, and further include an organosilicon compound represented by the following general formula (Formula 3) as a silica dispersant. 10 parts by weight or less, preferably 0.5 to 10 parts by weight, may be added to 100 parts by weight of the organopolysiloxane of the component (a).

【化3】 (ここで、Rc、Rdは前記Rと同じ炭素原子数1〜10の非
置換または置換の1価炭化水素基であり、但し脂肪族不
飽和炭化水素基、フッ素置換炭化水素基であってもよ
く、特にメチル基、ビニル基、フェニル基、3,3,3
−トリフルオロプロピル基が好ましい。bは1〜100 で
ある。)
Embedded image (Here, R c and R d are the same unsubstituted or substituted monovalent hydrocarbon groups having 1 to 10 carbon atoms as R, provided that they are aliphatic unsaturated hydrocarbon groups or fluorine-substituted hydrocarbon groups. And especially methyl, vinyl, phenyl, 3,3,3
-A trifluoropropyl group is preferred. b is 1 to 100. )

【0013】[0013]

【実施例】次に実施例を挙げるが、ここでは部は全て重
量部を示す。また物性測定値は以下の方法により測定し
た。
The following examples will be given, in which all parts are by weight. The measured physical properties were measured by the following methods.

【0014】(耐100 %伸長疲労寿命の測定法)デマッ
シャ式屈曲疲労試験機[東洋精機(株)製]を使用して
測定し、テストダンベルは JIS K6301,3項指定の3号ダ
ンベル、室温、5Hzで連続運転し破断までのサイクル数
を表示した。 (屈曲疲労による亀裂の成長速度の測定法)JIS K6301
に指定の屈曲疲労テストに準じてテストを行ない、予め
発生させておいた 2.5mmのクラックが室温、5Hzの屈曲
テストにおいて10mmになるまでの屈曲回数を求めた。
(Measurement method for 100% elongation fatigue life) Measured using a Demasher-type bending fatigue tester (manufactured by Toyo Seiki Co., Ltd.). The operation was continued at 5 Hz, and the number of cycles until breakage was displayed. (Measurement method of crack growth rate due to bending fatigue) JIS K6301
A bending test was performed according to the specified bending fatigue test, and the number of bendings until a 2.5 mm crack generated beforehand became 10 mm in a 5 Hz bending test at room temperature was determined.

【0015】(実施例1〜5;比較例1〜6)分子鎖両
末端が(CH3)2(CH2=CH)SiO-で、分子主鎖が全て−(CH3)2
SiO-単位からなるオルガノポリシロキサン95重量部、分
子鎖両末端が(CH3)2(CH2=CH)SiO-で、分子主鎖が−(C
H3)2SiO-単位が90モル%、-(CH3)(CH2=CH)SiO-単位が10
モル%からなるオルガノポリシロキサン5重量部、比表
面積が 200m2/gであるヒュームドシリカ・アエロジル20
0 [日本アエロジル製商品名]30重量部、シリカ分散剤
として分子鎖両末端がシラノール基で封鎖された重合度
約20のジメチルポリシロキサン8重量部をニーダーで混
練し、 170℃/2時間の熱処理をしてシリコーンゴム組
成物を調製した。
(Examples 1 to 5; Comparative Examples 1 to 6) Both ends of the molecular chain are (CH 3 ) 2 (CH 2 CHCH) SiO—, and all of the molecular main chains are — (CH 3 ) 2.
95 parts by weight of an organopolysiloxane composed of SiO- units, both ends of the molecular chain being (CH 3 ) 2 (CH 2 = CH) SiO-, and the molecular main chain being-(C
90 mol% of H 3 ) 2 SiO-units, 10-(CH 3 ) (CH 2 = CH) SiO-units
5% by weight of an organopolysiloxane consisting of mol% and a specific surface area of 200 m 2 / g fumed silica Aerosil 20
0 [trade name, manufactured by Nippon Aerosil Co., Ltd.] 30 parts by weight, and 8 parts by weight of dimethylpolysiloxane having a polymerization degree of about 20 in which both ends of a molecular chain are blocked with silanol groups as a silica dispersing agent are kneaded with a kneader, and the mixture is mixed at 170 ° C./2 hours Heat treatment was performed to prepare a silicone rubber composition.

【0016】更に架橋剤として、両末端がジメチルハイ
ドロジエンシリル基で封鎖され、その主鎖の20モル%が
-H(CH3)SiO-単位であり、その他は -(CH3)2SiO-単位で
あって、且つ重合度が表1に示される値のオルガノハイ
ドロジエンポリシロキサンを各々調製した。シリコーン
ゴム組成物中のオルガノポリシロキサンの1分子中に含
まれるビニル基のモル数を(SiVi)とし、上記オルガノ
ハイドロジエンポリシロキサン1分子中に含まれる SiH
基のモル数を(SiH)としたとき、モル比(SiH)/(SiVi)が
表1に示される値になるような量のオルガノハイドロジ
エンポリシロキサンを上記組成物に加えた。但し比較例
5のみ上記オルガノハイドロジェンポリシロキサンを加
えなかった。
Further, as a cross-linking agent, both terminals are blocked with a dimethylhydrogensilyl group, and 20 mol% of the main chain is
Organohydrogenpolysiloxanes each having -H (CH 3 ) SiO- units and-(CH 3 ) 2 SiO- units having the degree of polymerization shown in Table 1 were prepared. The number of moles of a vinyl group contained in one molecule of the organopolysiloxane in the silicone rubber composition is defined as (SiVi), and the number of moles of SiH contained in one molecule of the organohydrogenpolysiloxane is defined as (SiVi).
When the number of moles of the group was (SiH), the organohydrogenpolysiloxane was added to the composition in such an amount that the molar ratio (SiH) / (SiVi) became the value shown in Table 1. However, only the comparative example 5 did not contain the organohydrogenpolysiloxane.

【0017】また比較例5〜6ではパーオキサイド加硫
として表1の過酸化物を各々0.5 重量部添加した。但し
比較例6のみ白金触媒を添加しなかった。
In Comparative Examples 5 and 6, each of the peroxides shown in Table 1 was added in an amount of 0.5 part by weight as peroxide vulcanization. However, only the platinum catalyst was not added in Comparative Example 6.

【0018】実施例及び比較例の組成物に対して塩化白
金酸のオクチルアルコール変性溶液で白金量が2重量%
である白金触媒をそれぞれ 0.2重量部及び制御剤として
エチニルシクロヘキサノール0.05重量部を添加して本発
明の組成物及び比較例の組成物とし、これらをそれぞれ
2本ロールで混練し、 170℃/10分間プレスし、加硫し
た。耐伸長疲労測定用として2mm厚のシートを上記条件
で成形し、耐屈曲疲労測定用としては JIS K6301に準じ
て成形した。これらについて前記2種類の試験を実施
し、得られた結果を表2に示した。本発明の組成物の硬
化物は耐伸長疲労性及び耐屈曲疲労性に優れていること
が明らかになった。
The amount of platinum was 2% by weight in the octyl alcohol-modified solution of chloroplatinic acid with respect to the compositions of Examples and Comparative Examples.
Was added to the composition of the present invention and the composition of the comparative example by adding 0.2 parts by weight of a platinum catalyst and 0.05 part by weight of ethynylcyclohexanol as a control agent. Pressed for minutes and vulcanized. A sheet having a thickness of 2 mm was formed under the above-mentioned conditions for elongation fatigue resistance measurement, and was formed in accordance with JIS K6301 for bending fatigue resistance measurement. These two types of tests were performed on these, and the obtained results are shown in Table 2. It became clear that the cured product of the composition of the present invention was excellent in elongation fatigue resistance and flex fatigue resistance.

【0019】[0019]

【表1】 [Table 1]

【0020】[0020]

【表2】 [Table 2]

【0021】[0021]

【発明の効果】耐屈曲疲労特性、特にクラックの成長速
度の非常に遅い、且つ耐伸長疲労特性に優れた自動車ジ
ョイントカバーブーツ用のシリコーンゴム組成物を提供
することができる。
As described above, it is possible to provide a silicone rubber composition for automobile joint cover boots having excellent bending fatigue resistance, particularly a very low crack growth rate, and excellent extension fatigue resistance.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 下記イ)、ロ)、ハ)、ニ)からなる自
動車ジョイントカバーブーツ用シリコーンゴム組成物。 イ)平均組成式RaSiO(4-a)/2で示され、1分子中に少なくとも2個の脂肪族不飽 和炭化水素基を有するオルガノポリシロキサン 100重量部、 (但し式中R は置換または非置換の一価炭化水素基で、aは1.95〜2.05の正数) ロ)下記一般式(化1)で示され、1分子中にケイ素原子に結合した水素原子を 少なくとも2個有するオルガノハイドロジエンポリシロキサン 「但しロ)の 水素原子のモル数とイ)の脂肪族不飽和炭化水素基のモル数との比が 1.0〜2.5 となる重量部」、 「式中R は前記と同じ,A はH またはR ,B はSiRH2,SiR2H,SiR3から選ばれる基 ,mはm≧0の整数,nはn≧0の整数で且つ5≦(m+n)≦100 」 【化1】 ハ)補強性シリカ 10〜 100重量部、 ニ)白金系触媒 触媒量。
1. A silicone rubber composition for automobile joint cover boots comprising the following a), b), c) and d). A) 100 parts by weight of an organopolysiloxane represented by the average composition formula R a SiO (4-a) / 2 and having at least two aliphatic unsaturated hydrocarbon groups in one molecule, wherein R is A is a substituted or unsubstituted monovalent hydrocarbon group, a is a positive number from 1.95 to 2.05) b) is represented by the following general formula (Formula 1) and has at least two hydrogen atoms bonded to silicon atoms in one molecule Organohydrogenpolysiloxane "where the ratio of the number of moles of hydrogen atoms in b) to the number of moles of aliphatic unsaturated hydrocarbon groups in b) is 1.0 to 2.5", wherein R is the same as defined above. , a is H or R, B is SiRH 2, SiR 2 H, a group selected from SiR 3, m is an integer of m ≧ 0, n is and integer of n ≧ 0 5 ≦ (m + n) ≦ 100 "embedded 1) C) Reinforcing silica 10 to 100 parts by weight, d) Platinum catalyst Catalyst amount.
【請求項2】 分子鎖末端が脂肪族不飽和炭化水素基で
あり、その平均組成式におけるRの0.25〜10モル%が脂
肪族不飽和炭化水素基であるイ)のオルガノポリシロキ
サン 0.5〜30重量部をオルガノポリシロキサン100 重量
部中に含有することを特徴とする請求項1記載の自動車
ジョイントカバーブーツ用シリコーンゴム組成物。
2. The organopolysiloxane of a) wherein the molecular chain terminal is an aliphatic unsaturated hydrocarbon group and 0.25 to 10 mol% of R in the average composition formula is an aliphatic unsaturated hydrocarbon group. 2. The silicone rubber composition for automobile joint cover boots according to claim 1, wherein parts by weight are contained in 100 parts by weight of the organopolysiloxane.
JP8321557A 1996-12-02 1996-12-02 Silicone rubber composition for automobile joint cover Pending JPH10158518A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP8321557A JPH10158518A (en) 1996-12-02 1996-12-02 Silicone rubber composition for automobile joint cover

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP8321557A JPH10158518A (en) 1996-12-02 1996-12-02 Silicone rubber composition for automobile joint cover

Publications (1)

Publication Number Publication Date
JPH10158518A true JPH10158518A (en) 1998-06-16

Family

ID=18133903

Family Applications (1)

Application Number Title Priority Date Filing Date
JP8321557A Pending JPH10158518A (en) 1996-12-02 1996-12-02 Silicone rubber composition for automobile joint cover

Country Status (1)

Country Link
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JP2013190042A (en) * 2012-03-14 2013-09-26 Ntn Corp Constant velocity universal joint boot
JP2020143259A (en) * 2019-03-08 2020-09-10 住友ベークライト株式会社 Silicone rubber-based curable composition and wearable device using the same
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Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001234875A (en) * 2000-02-22 2001-08-31 Seiko Epson Corp Tube pump and ink jet type recording device using it
WO2013137128A1 (en) * 2012-03-14 2013-09-19 Ntn株式会社 Constant velocity universal joint
JP2013190034A (en) * 2012-03-14 2013-09-26 Ntn Corp Constant velocity universal joint
JP2013190042A (en) * 2012-03-14 2013-09-26 Ntn Corp Constant velocity universal joint boot
US9181986B2 (en) 2012-03-14 2015-11-10 Ntn Corporation Constant velocity universal joint
JP2020143259A (en) * 2019-03-08 2020-09-10 住友ベークライト株式会社 Silicone rubber-based curable composition and wearable device using the same
JP2020143244A (en) * 2019-03-08 2020-09-10 住友ベークライト株式会社 Silicone rubber-based curable composition and structure comprising the same
WO2020183969A1 (en) * 2019-03-08 2020-09-17 住友ベークライト株式会社 Silicone-rubber-based curable composition, structure, wearable device, and method for manufacturing structure
CN113614175A (en) * 2019-03-08 2021-11-05 住友电木株式会社 Silicone rubber-based curable composition, structure, wearable device, and method for producing structure
KR20210137112A (en) * 2019-03-08 2021-11-17 스미또모 베이크라이트 가부시키가이샤 Silicone rubber-based curable composition, structure, wearable device, and method of manufacturing the structure

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